Liu Jin, Shi Qiuyan, Sun Yuan, He Jingyuan, Yang Bin, Zhang Chunyang, Guo Rui
Department of Neurology, Affiliated Hospital of North China University of Science and Technology, Tangshan 063000, China.
J Stroke Cerebrovasc Dis. 2019 Apr;28(4):1126-1132. doi: 10.1016/j.jstrokecerebrovasdis.2018.12.044. Epub 2019 Jan 14.
To evaluate the efficacy of tirofiban administered at different time points within 24 hours of intravenous thrombolysis with alteplase in acute ischemic stroke.
Patients who underwent intravenous thrombolysis with alteplase and fulfilled other inclusion criteria were randomly divided into 4 groups according to the time points of tirofiban administration: Group A (2 h), Group B (2-12 h), Group C (12-24 h), and Group D (control). The changes in National Institutes of Health Stroke Scale score, modified Rankin Scale score, and adverse events were analyzed.
At 7 ± 1 day, the efficacy in Group A was better than that in Group C (P = .006) and Group D (P = .001), but there was no significant difference in the efficacy between Groups A and B (P = .268). Similarly, at 14 ± 2 d, the efficacy in Group A was better than that in Group C (P = .026) and Group D (P = .001), but there was no significant difference in the efficacy between Groups A and B (P = .394). As evaluated by the modified Rankin Scale, the prognosis in Groups A, B, and C was better than that in Group D (P = .042, .008, .027, respectively), which was unrelated to the time points of tirofiban administration. There was no significant difference in the incidence of adverse events among the four groups.
Tirofiban combined with alteplase is effective and safe, and particularly beneficial when administered at 2 hour and 2-12 hours after intravenous thrombolysis with alteplase in acute ischemic stroke.
评估替罗非班在急性缺血性卒中患者静脉注射阿替普酶后24小时内不同时间点给药的疗效。
接受阿替普酶静脉溶栓且符合其他纳入标准的患者,根据替罗非班给药时间点随机分为4组:A组(2小时)、B组(2 - 12小时)、C组(12 - 24小时)和D组(对照组)。分析美国国立卫生研究院卒中量表评分、改良Rankin量表评分及不良事件的变化。
在7±1天时,A组疗效优于C组(P = 0.006)和D组(P = 0.001),但A组与B组疗效差异无统计学意义(P = 0.268)。同样,在14±2天时,A组疗效优于C组(P = 0.026)和D组(P = 0.001),但A组与B组疗效差异无统计学意义(P = 0.394)。根据改良Rankin量表评估,A、B、C组的预后均优于D组(分别为P = 0.042、0.008、0.027),且与替罗非班给药时间点无关。四组不良事件发生率差异无统计学意义。
替罗非班联合阿替普酶有效且安全,尤其在急性缺血性卒中患者静脉注射阿替普酶后2小时及2 - 12小时给药时更有益。